2-Methylbutyryl-Co A Dehydrogenase Deficiency
2-Methylbutyryl-CoA dehydrogenase deficiency, also called 2-Methylbutyryl glycinuria or short/branched-chain acyl-CoA dehydrogenase deficiency (SBCADD), is an autosomal recessive metabolic disorder. It causes the body to be unable to process the amino acid isoleucine properly.
Read more about 2-Methylbutyryl-Co A Dehydrogenase Deficiency: Signs and Symptoms, Cause and Genetics
Famous quotes containing the word deficiency:
“It is easier to discover a deficiency in individuals, in states, and in Providence, than to see their real import and value.”
—Georg Wilhelm Friedrich Hegel (1770–1831)